Method for increasing acid production rate and extracting rate of glutamic acid
A technology of glutamic acid and acid production rate, which is applied in microorganism-based methods, chemical instruments and methods, biochemical equipment and methods, etc. problems, to achieve the effect of saving raw material expenses, retaining nutritional value, and reducing high pigment content
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Embodiment 1
[0031] An amino acid fermentation medium, which includes a fermentation medium A and a fermentation medium B, the fermentation medium A and the fermentation medium B are used separately, and the amino acid is glutamic acid;
[0032] The fermentation medium B is to add inositol and glycerol on the basis of the fermentation medium A;
[0033] The fermentation medium A is: glucose 50g / L, Na 2 HPO 4 12H 2 O 2g / L, KCl 1g / L, MgSO 4 ·7H 2 O 1g / L, MnSO 4 ·H 2 O 3mg / L, FeSO 4 ·7H 2 O 3mg / L, V B1 10mg / L, 1mg / L fulvic acid, 7μg / L biotin, 60ml / L enzymatic hydrolyzate, sterilized at 115°C for 15min;
[0034]The fermentation medium B is: glucose 50g / L, Na 2 HPO 4 12H 2 O 2g / L, KCl 1g / L, MgSO 4 ·7H 2 O 1g / L, MnSO 4 ·H 2 O 3mg / L, FeSO 4 ·7H 2 O 3mg / L, V B1 10mg / L, 1mg / L fulvic acid, 7μg / L biotin, 60ml / L cell enzymolysis solution, 100mg / L inositol, 500mg / L glycerin, sterilized at 115°C for 15min;
[0035] The preparation method of the thallus enzymatic solution is as follow...
Embodiment 2
[0038] A method for improving the acid production rate and extraction rate of glutamic acid, comprising the steps of:
[0039] Brevibacterium flavum GDK-9 (sourced from Tianjin University of Science and Technology, see "Study on variable temperature control process of L-glutamic acid fermentation, Tianjin Chemical Industry Co., Ltd., 2010" for the source of the strain) was inoculated with 12% seed solution (OD 600nm 10) Connect to a 50L automatic fermenter equipped with 30L fermentation medium A for fermentation and cultivation, the fermentation temperature is 38°C, the ventilation ratio is 1:0.7, the stirring speed is 500r / min, and the dissolved oxygen is maintained at 20%. Coupled with a ceramic membrane, when the fermentation lasts to 24 hours, the fermentation liquid in the fermenter is separated through a ceramic membrane (molecular weight cut-off is 20000Da), the filtrate is discharged, the concentrated bacteria are returned to the fermenter, and at the same time, additio...
Embodiment 3
[0041] Influence of hydrolysis process on bacterial proteolysis components:
[0042] Set up a control group,
[0043] Matched group 1: do not adopt high-speed shearing machine to process, all the other are the same as embodiment 1;
[0044] Control group 2: Hydrochloric acid with a concentration of 5 mol / L was used for hydrolysis for 6 hours.
[0045] The wall breaking rate, protein content and total free amino acid content are shown in Table 1:
[0046] group
Example 1
Control group 1
Control group 2
Broken rate%
97.2
83.4
68.7
Protein content mg / g (dried bacteria)
226.1
285.9
268.5
Total free amino acid content mg / g (dried bacteria)
371.5
256.3
187.4
[0047] Visible by table 1, utilize high-speed shearing machine to shear and process 120s, can greatly improve cell wall breaking rate, thereby improve hydrolysis efficiency; The present invention adopts dilute hydrochloric acid to carry out pretreatmen...
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